Observational Biologic or Prosthetic Mesh

Stopped early

Conditions studied: Ventral Incisional Hernia

In brief

The purpose of this study is to assess the incidence of hernia recurrence with the use of biologic and prosthetic mesh in ventral hernia repair.

Key facts

Study ID

NCT03317665

Run by

University of South Florida

People needed

28

Starts

2019-02-11

Expected to finish

2021-06-11

Last updated by the study team

2021-10-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female patients > 21 years old.
• Able to provide informed consent in English or Spanish.
• Stated willingness to comply with all study procedures and availability for the duration of the study.

You may not qualify if…

• Pregnant, breastfeeding, or unwilling to practice birth control during participation in the study, if applicable.
• Allergy or hypersensitivity to materials in porcine-based study products, prosthetic or biological meshes, or personal preference.
• Male and female patients ≤ 21 years old
• History of drug addiction (recreational drugs, prescription drugs or alcohol) that in the Investigator's opinion may interfere with protocol assessments and/or the subject's ability to complete the required follow up.
• Serious or active medical or psychiatric condition which, in the opinion of the Investigator, may interfere with treatment, assessment, or compliance with the protocol.

Where it is running

• Tampa General Hospital — Tampa, Florida, United States
• University of South Florida - South Tampa Campus — Tampa, Florida, United States
• University of South Florida Morsani Center for Advanced Health Care — Tampa, Florida, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.